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GM00336 Fibroblast

Description:

GALACTOKINASE DEFICIENCY
GALACTOKINASE 1; GALK1

Affected:

No Data

Sex:

Male

Age:

62 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Images
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Class Disorders of Carbohydrate Metabolism
Cell Type Fibroblast
Transformant Untransformed
Race White
Family Member 3
Relation to Proband father
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Passage 4 at CCR; 79% of control galactokinase activity in fibroblasts; clinically unaffected father of GM00334A

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase Isoenzyme Electrophoresis
 
galactokinase According to the submitter, biochemical test results for this subject showed decreased enzyme activity. EC Number: 2.7.1.6; 79% activity.
 
Gene GALK1
Chromosomal Location 17q25.1
Allelic Variant 1 604313.0001; GALACTOKINASE DEFICIENCY WITH CATARACTS
Identified Mutation VAL32MET; In family GB in which the proband had galactokinase deficiency and congenital cataracts, Stambolian et al. (1995) found a single base substitution of A for G at position 94, which resulted in a val32-to-met substitution.

Phenotypic Data

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Remarks Passage 4 at CCR; 79% of control galactokinase activity in fibroblasts; clinically unaffected father of GM00334A

Publications

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Stambolian D, Ai Y, Sidjanin D, Nesburn K, Sathe G, Rosenberg M, Bergsma DJ, Cloning of the galactokinase cDNA and identification of mutations in two families with cataracts. Nat Genet10:307-12 1995
PubMed ID: 7670469
 
Stephenson C, Brivet M, Gautier M, Deschatrette J, Gitzelmann R, Karran P, Normal expression of thymidine kinase and O6-methylguanine-DNA methyltransferase in cultured fibroblasts from individuals with hereditary galactokinase deficiency. Biochem Genet29:135-44 1991
PubMed ID: 1859354
 
Schoen RC, Cox SH, Wagner RP, Thymidine-kinase activity of cultured cells from individuals with inherited galactokinase deficiency. Am J Hum Genet36:815-22 1984
PubMed ID: 6475956
 
Friedman TB, Yarkin RJ, Merril CR, Galactose and glucose metabolism in galactokinase deficient, galactose- 1-P-uridyl transferase deficient and normal human fibroblasts. J Cell Physiol85:569-78 1975
PubMed ID: 167035

External Links

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dbSNP dbSNP ID: 15653
Gene Cards GALK1
Gene Ontology GO:0004335 galactokinase activity
GO:0005524 ATP binding
GO:0005737 cytoplasm
GO:0006012 galactose metabolism
GO:0008152 metabolism
GO:0016301 kinase activity
GO:0016310 phosphorylation
GO:0016740 transferase activity
NCBI Gene Gene ID:2584
NCBI GTR 230200 GALACTOSEMIA II; GALAC2
604313 GALACTOKINASE 1; GALK1
OMIM 230200 GALACTOSEMIA II; GALAC2
604313 GALACTOKINASE 1; GALK1
Omim Description GALACTOKINASE DEFICIENCY
  GALACTOSEMIA IIGALACTOKINASE 1; GALK1, INCLUDED
  GALK DEFICIENCY
  GK1, INCLUDED

Images

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View pedigree 

Culture Protocols

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Split Ratio 1:3
Temperature 37 C
Percent CO2 5%
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not inactivated
Substrate None specified
Subcultivation Method trypsin-EDTA
Supplement -
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International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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